| Title : The clinical and molecular landscape of congenital myasthenic syndromes in Austria: a nationwide study - Krenn_2022_J.Neurol__ |
| Author(s) : Krenn M , Sener M , Rath J , Zulehner G , Keritam O , Wagner M , Laccone F , Iglseder S , Marte S , Baumgartner M , Eisenkolbl A , Liechtenstein C , Rudnik S , Quasthoff S , Grinzinger S , Spenger J , Wortmann SB , Loscher WN , Zimprich F , Kellersmann A , Rappold M , Bernert G , Freilinger M , Cetin H |
| Ref : Journal of Neurology , : , 2022 |
| Abstract : |
| PubMedSearch : Krenn_2022_J.Neurol__ |
| PubMedID: 36308527 |
| Title : Treatment of volanesorsen in a patient with familial chylmicronaemia syndrome (FCS) due to homozygous c.337T>C(p.TRP113ARG) - mutation and impact of dietary incompliance: A case report - De Gier_2022_Atherosclerosis_355_65 |
| Author(s) : De Gier C , Skacel G , Walleczek NK , Lischka J , Baumgartner M , Greber-Platzer S |
| Ref : Atherosclerosis , 355 :65 , 2022 |
| Abstract : |
| PubMedSearch : De Gier_2022_Atherosclerosis_355_65 |
| PubMedID: |
| Gene_locus related to this paper: human-LPL |
| Title : The clinical and molecular landscape of congenital myasthenic syndromes in Austria: a nationwide study - Krenn_2022_J.Neurol__ |
| Author(s) : Krenn M , Sener M , Rath J , Zulehner G , Keritam O , Wagner M , Laccone F , Iglseder S , Marte S , Baumgartner M , Eisenkolbl A , Liechtenstein C , Rudnik S , Quasthoff S , Grinzinger S , Spenger J , Wortmann SB , Loscher WN , Zimprich F , Kellersmann A , Rappold M , Bernert G , Freilinger M , Cetin H |
| Ref : Journal of Neurology , : , 2022 |
| Abstract : |
| PubMedSearch : Krenn_2022_J.Neurol__ |
| PubMedID: 36308527 |
| Title : The clinical and molecular landscape of congenital myasthenic syndromes in Austria: a nationwide study - Krenn_2022_J.Neurol__ |
| Author(s) : Krenn M , Sener M , Rath J , Zulehner G , Keritam O , Wagner M , Laccone F , Iglseder S , Marte S , Baumgartner M , Eisenkolbl A , Liechtenstein C , Rudnik S , Quasthoff S , Grinzinger S , Spenger J , Wortmann SB , Loscher WN , Zimprich F , Kellersmann A , Rappold M , Bernert G , Freilinger M , Cetin H |
| Ref : Journal of Neurology , : , 2022 |
| Abstract : |
| PubMedSearch : Krenn_2022_J.Neurol__ |
| PubMedID: 36308527 |
| Title : Treatment of volanesorsen in a patient with familial chylmicronaemia syndrome (FCS) due to homozygous c.337T>C(p.TRP113ARG) - mutation and impact of dietary incompliance: A case report - De Gier_2022_Atherosclerosis_355_65 |
| Author(s) : De Gier C , Skacel G , Walleczek NK , Lischka J , Baumgartner M , Greber-Platzer S |
| Ref : Atherosclerosis , 355 :65 , 2022 |
| Abstract : |
| PubMedSearch : De Gier_2022_Atherosclerosis_355_65 |
| PubMedID: |
| Gene_locus related to this paper: human-LPL |
| Title : Treatment of volanesorsen in a patient with familial chylmicronaemia syndrome (FCS) due to homozygous c.337T>C(p.TRP113ARG) - mutation and impact of dietary incompliance: A case report - De Gier_2022_Atherosclerosis_355_65 |
| Author(s) : De Gier C , Skacel G , Walleczek NK , Lischka J , Baumgartner M , Greber-Platzer S |
| Ref : Atherosclerosis , 355 :65 , 2022 |
| Abstract : |
| PubMedSearch : De Gier_2022_Atherosclerosis_355_65 |
| PubMedID: |
| Gene_locus related to this paper: human-LPL |